Single‐Molecule Localization Microscopy Using Time‐Lapse Imaging of Single‐Antibody Labeling

Abstract

AbstractIn single‐molecule localization microscopy (SMLM), immunofluorescence (IF) staining affects the quality of the reconstructed superresolution images. However, optimizing IF staining remains challenging because IF staining is a one‐step, irreversible process. Sample labeling through reversible binding presents an alternative strategy, but such techniques require significant technological advancements to enhance the dissociation of labels without sacrificing their binding specificity. In this article, we introduce time‐lapse imaging of single‐antibody labeling. Our versatile technique utilizes commercially available dye‐conjugated antibodies. The method controls the antibody concentrations to capture single‐antibody labeling of subcellular targets, thereby achieving SMLM through the labeling process. We further demonstrate dual‐color single‐antibody labeling to enhance the sample labeling density. The new approach allows the evaluation of antibody binding at the single‐antibody level and within the cellular environment. This comprehensive guide offers step‐by‐step instructions for time‐lapse imaging of single‐antibody labeling experiments and enables the application of the single‐antibody labeling technique to a wide range of targets. © 2023 The Authors. Current Protocols published by Wiley Periodicals LLC.Basic Protocol 1: Sample preparation for single‐antibody labelingBasic Protocol 2: Data acquisition for single‐molecule localization microscopyAlternate Protocol: Dual‐color single‐antibody labeling using OptoSplit II equationBasic Protocol 3: Image analysis